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Clinical Evaluation of a Self-Adhering Flowable Composite in Class I Cavities

Not Applicable
Completed
Conditions
Tooth Diseases
Interventions
Device: Vertise Flow
Device: LuxaFlow
Device: Teco Adhesive
Registration Number
NCT03556553
Lead Sponsor
Hacettepe University
Brief Summary

The aim of this study is to evaluate long-term clinical performance of a self-adhering flowable resin composite in comparison with a conventional flowable resin composite used with an etch\&rinse adhesive system in minimally invasive class I cavities. Twenty-five patients will receive at least one pair of class I restorations. After class I cavities were prepared they were restored either with a self-adhering flowable resin composite (VertiseFlow/Kerr-VR) or with a flowable resin composite (Luxaflow/DMG-LX) in combination with an etch\&rinse adhesive (Teco/DMG) \[according to the manufacturers' instructions. Restorations will be evaluated at baseline and yearly according to FDI criteria by two evaluaters. Statistical analysis will be carried out with Pearson Chi-Square test and Cochran Q-test followed by Mc Nemar's.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
Inclusion Criteria
  • having no medical or behavioral problems preventing then from attending review visits, absence of previously placed restorations,having antagonist teeth
Exclusion Criteria
  • poor gingival health,uncontrolled, rampant caries,bruxism,removable partial dentures, xerostomia

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Vertise FlowVertise FlowSuperficial Class I cavities restored with Vertise Flow
LuxaFlowTeco AdhesiveSuperficial Class I cavities restored with LuxaFlow
LuxaFlowLuxaFlowSuperficial Class I cavities restored with LuxaFlow
Primary Outcome Measures
NameTimeMethod
Clinical performances of flowable composite resinsFive years

Five year results according to FDIcriteria

Secondary Outcome Measures
NameTimeMethod
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